Comparison of Colon Adenoma Detection Rate Using Two Distal Colonoscope Attachments (NCT02665741) | Clinical Trial Compass
CompletedNot Applicable
Comparison of Colon Adenoma Detection Rate Using Two Distal Colonoscope Attachments
United States126 participantsStarted 2016-01
Plain-language summary
The goal of this study is to compare two FDA approved distal colonoscope attachment devices, in order to identify which device can increase adenoma detection rate the most without increasing procedure time or risk.
Who can participate
Age range50 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* At least 50 years old
* Presenting for a screening or surveillance colonoscopy at UC Davis Endoscopy Suites
Exclusion Criteria:
* Age less than 50 years
* Prior history of colon cancer
* Patients with inflammatory bowel disease
* Patients suspected to have colon cancer based on non invasive tests such as stool tests for hemoglobin or DNA, or imaging finding suggestive of colon cancer (CT or barium enema).
* Patients undergoing colonoscopy for evaluation of symptoms such as abdominal pain, rectal bleeding, diarrhea, constipation, etc, or patient with iron deficiency anemia suspected to be due to ongoing bleeding inside the colon
* Patients with family history of colon cancer in 1st degree relative below the age of 60
* Patients with family history of hereditary polyposis syndromes such as Lynch syndrome, familial adenomatous polyposis etc, which are associated with an increased risk of colon cancer
* Patients unable to consent
* Pregnant patients
* Incarcerated patients
* Non-English speakers